Tim Truth lost me a long time ago with some of the bullshit he was spouting.
When he and Agent..... something or other, decided to smear vitamin D3, methylene blue and Ivermectin, it just reinforced my very low opinion of these clowns.
I used to read and watch some of his stuff before he started his "ivermectin is poison" campaign. As soon as he started that- i stopped. There's something not right about it and it makes me wonder how much $ it took for him to smear ivermectin, quercitin, vitamin D, etc...
Big Pharma goal for many decades has been to discredit any treatment module or diagnostic module or nutritional module that is cheap and effective! In the US you don’t become one half Trillion dollar industry any other way! Now custom targeted expensive chemo/cancer treatment and RNA injections will expand the industry to a Trillion dollars!
A Save The Narrative campaign by the Save Our Asses crew ... as the truth spreads awakening the sleepy-near-dead all efforts - especially censorship as is being passed by complicit U.S. Govt. - are ramped up, to reinforce and beef up the original implanted nonsense. Anything to stop public lynching. Can it be stopped? Time to buy stock in rope's raw material.
Hi Smartest off topic but thought you might like it..
💥
HUMAN CHALLENGE TRIAL FAIL 2024
Scientists tried to give people COVID — and failed
Researchers deliberately infect participants with SARS-CoV-2 in ‘challenge’ trials — but high levels of immunity complicate efforts to test vaccines and treatments.
Immunological memory is the ability of the immune system to quickly and specifically recognize an antigen that the body has previously encountered and initiate a corresponding immune response. Generally these are secondary, tertiary and other subsequent immune responses to the same antigen. Immunological memory is responsible for the adaptive component of the immune system, special T and B cells — the so-called memory T and B cells.
.
IgG antibodies are Y-shaped protein molecules that are produced by special white blood cells (B lymphocytes) in response to foreign substances (antigens) such as viruses or bacteria. Antibodies can attach to these viruses or bacteria, rendering them harmless and unable to penetrate healthy cells. They GO AWAY with time and could fall to a NEGATIVE level DOESN'T mean susceptible.
.
Total immunity against viral diseases includes:
1. Local IgA and IgM
2. Humoral immunity of IgG antibodies, both those present in the blood AND those that can be produced quickly when the antigen is present
3. Cellular immunity or MEMORY
4. Other mechanisms.
When we measure antibody titers, we are ONLY documenting the IgG antibodies present in the bloodstream.
.
The Immune System fires up when a pathogen, like a virus, enters the body. The pathogen releases a protein called an antigen, which calls into action the immune system’s special disease-fighting cells. "Called B and T lymphocytes", these cells NOT only destroy the virus, but they REMEMBER what it looked like so they can fend it off in the FUTURE.
.
IMMUNOLOGIC MEMORY allows the immune system to REMEMBER the antigens or organisms to which it has previously been exposed. MEMORY EFFECTOR B cells (long-lived plasma cells) and MEMORY T-cells specific to a virus, give long-term immunity against these diseases.
.
ADAPTIVE IMMUNITY.
.
The “Adaptive Immune Response" is younger than the “Innate Immune Response" in evolutionary terms and is more specific and considerably MORE POTENT in its effects.
.
The constituents of the adaptive immune response are the lymphoid cells. These include:
.
The T lymphocytes and the cytokine and chemokine messenger proteins released by these cells, which direct and REGULATE the adaptive immune response.
.
The B lymphocytes, which transform to the late-stage plasma cells that produce and secrete antibody.
.
The lymphoid cells of the adaptive immune response reside in, and circulate between, the various lymphoid tissues of the body (e.g. the lymph nodes, spleen and mucosal lymphoid tissues). In the adaptive immune response, antigen is first transported from a site of infection by a dendritic cell to the regional lymphoid tissue. That dendritic cell in turn activates "Antigen-Specific T lymphocytes," which further activate Antigen-Specific B lymphocytes.”
.
These activated, Antigen-Specific lymphocytes must then be mobilized from the regional lymphoid tissue and sent to the site of infection, a process that involves these cells moving into the lymphatic and blood circulation and interacting with the endothelial lining of blood vessels.
.
Once these cells reach the site of infection, they are able to mount a full-scale ‘EFFECTOR’ response, which is considerably STRONGER than that permitted by innate immunity. As these processes take some time to occur (in the order of 4–7 days), there is a delay before adaptive immunity ‘takes over’ from the innate form of defence.
.
The final component of Adaptive Immunity is the development of a “REGULATORY RESPONSE" that will "SWITCH OFF" the system when it is NO LONGER REQUIRED (i.e. when the pathogen has been ELIMINATED) so as NOT to cause DAMAGE to normal body tissue.
.
HOWEVER, once this is achieved, the immune system retains the “MEMORY” of that immune response.
IMMUNOLOGICAL MEMORY is another key feature of the Adaptive Immune Response. MEMORY allows the generation of a much MORE effective SECONDARY IMMUNE RESPONSE (Anamnestic MEMORY Response) if that same antigen is EVER RE-ENCOUNTERED.
Thank yo! Well explained. Give all physicians a test on this before licensing! So..why does the medicine man not focus on improving immune system response in immune compromised humans.
My wife acquired B cell lymphoma. The Mayo researcher said they didn't have a clue why the B Cells attack the T cells that normally stop the viral invasion. Took ten years before the LDH went through the roof.
Used to subscribe to Celia, but then cut it off maybe over a year ago. I don't recall why but something about her writing/viewpoint not being well thought out...
Saw Celia's article yesterday, was a little surprised about it. Usually she is on top of most things but I don't follow Tim Truth either. Some of the comments on her article are worth the read as well. Linking your article today @https://nothingnewunderthesun2016.com/
I just saw what he is saying about ivermectin and also fenbenzedole, saying it's cockroach poison. What the fuck is going on, I'm assuming he's a pharma shill, trying to disparage a nobel prize winning drug. It's had billions of doses supplies and I've read it's safer than Panadol, is this true. Someone please help
Why would you need help? Billions of doses administered with virtually no side effects considered safer than tylenol. Clearly this person has an agenda alligned with the Elites that control Pharma "they want you dead" hence treatments that help are disparaged, this same clown also claims Quercetin is dangerous nd no doubt vitamin D and C are "dangerous" do you not see the pattern?
Ivermectin sounds very promising and has received a lot of publicity. However, it is still a Big Pharma product controlled by Big Pharma! I guess the question we have to ask ourselves is why they are still allowing it to be sold on the open market to the masses to use off-label as opposed to Hydroxycholoroquine and other off-label medications that were suggested during the Plandemic? I have zero trust in Big Pharma and the U.S. Medical System!
Ivermectin was first sold on the open market in the early 1980s at a time when pharma was actually producing useful compounds conicidentally Fenbendazole another antiparasitic also came out at that time. Both were initally used as an antiparasitics for animals and later repuprosed for humans. In Fenbendazole's case an entirely neutral sulfur subsititution was deployed and renamed mebendzole so the same thing could be sold for thousands of dollars per dose.
Ivermectin and Fenbendazole research for efficacy in other diseases including antiviral or even anticancer properties typically had good in vitro results good in vivo results (in animals) and then research stopped----Big pharmas mantra No Profit=No Product.
These drugs are now off patent and big pharma has actively tried to prevent them being repurposed for off label use.
Merck went as far as trying to purchase all the Ivermectin production facilities in India that turned into a game of whack a mole as one facility would be bought out and another set up. This has ZERO to do with big pharma who have actively tried to prevent the off label use of these compounds.
So to answer to your question repurposed off patent drugs thankfully are not in big pharma's control as described above. If you want to put big pharma out of business buy these life saving compounds as they represent to big pharma cheaper better products that actually work! Complete antithetical to big pharma's goals.
Thanks for clarifying that, Sid. I understand that they are also touting it as a cure for Cancer; however, I think a much better and much safer alternative to any pharmaceutical is Hemp Oil (composed of THC, CBD, and CBG), not to be confused with Hemp Seed Oil which has the best healing and Cancer curing properties. In his book "Nature's Answer to Cancer" Rick Simpson discusses his frustration with the Canadian medical system in treating his Cancer until he discovered Hemp Oil. Rick Simpson took it upon himself to opt out of conventional therapy with chemo and dangerous Big Pharma drugs and treated himself with his homemade hemp oil. He used his oil to treat thousands of Canadians suffering from Cancer and other serious health issues with his oil for Free. The result was that the Canadian government wanted to put him in prison. That in itself proves how well Hemp Oil works!
CBD oil is one of the components of the new and improved Tippens protocol, but it is not enough on its own.
There is a new full spectrum organic CBD product launching soon on this Substack which will be the most potent offering available, and at the most affordable price-point.
With all due respect, 2nd Smartest Guy, I have witnessed the Rick Simpson Oil for myself work wonders; Rick Simpson documented his results for THC/CBD oil before anyone even knew what CBD oil was. I just started making this oil for myself (circled back to the CBD "wagon") and my wife; it is fantastic. The stuff (junk) on the market is mass-produced and does not use the decarboxylation method to release the actual CBD, THC, CBG, and Terpene profile to get the same effect as the active ingredients in the hemp plant. The stuff on the market is mass-produced and is filtered with olive oil as a carrier. The Hemp has to be stripped of the trichome with either a solvent (200-proof food-grade alcohol), CO2, or Butane. Solvents are the best and then decarboxylated by dissolving the solvent at an optimal temperature without denaturing the CBD, THC, and CBG.
With all due respect IVM is easily one of the safest compounds out there. Given that many dissident Dr's in my case molecular biologist at risk to our careers spoke out about the anticancer properties of this compound "touting" is a really unfair characterization.
That being said it is very naive to think that any single compound is a "magic" bullet. I am a strong proponent of the "warburg" effect that states that cancer cells effectively rely on glucose instead of oxygen to store energy in the form of lactate. By making this in effect a therapeutic target calls for an integrative approach to this disease that includes a sugar restricted diet (I found substituting allulose (a rare sugar that is not metabolized) for regular sugar works great at starving cancer cells.
As a caregiver for a patient who happened to be a close relative I was able to bring stage 3 Multiple myeloma with a grim prognosis of only a few months to 100 percent full remission in seven months much to the chagrin of the Moffit cancer centre that my relative rejected their toxic chemothrapy but I digress,
Several steps were crucial;
1) he loved wine at least a bottle a day so I substituted wine for canaboid Oil being aware of the anticancer properties you refer to and as it was medicinal cannaboid oil that he had to register as a patient in Florida to obtain it helped relieve his anxieties.
2) Keto like diet
3) Fenbendazole 500 Mg daily.
4) Quercetin (konwn anti MM properties 2000 mg a day)
5) Vitamin d3 20000 Iu daily vital for bone health for MM patients Moffit center totally ignored this
This integrative approach worked. Additionally I know of at least one other patient that did a similar course of action except had IVM instead of Quercetin( 24 mg a day.) Also a patient that was at deaths door.
"Magic bullet" approach has a lower probability of working than an integratve approach.
Bravo; that is a beautiful recipe for healing! I am not well versed on the Ivermectin and I was out of the medical industry after twenty four plus years by December of 2020! We were one of the first medical clinics in my area at the time that would provide the medical marijuana recommendations.
Yes, fantastic stuff; I sleep like I did when I was seventeen! Any aches and pains melt away, and stress levels are at zero! The stuff that I use is low in THC 0.5% and the CBD is 17%. Rick Simpson recommends 17% THC for patients with cancers, especially advanced cancers!
Tim Truth lost me a long time ago with some of the bullshit he was spouting.
When he and Agent..... something or other, decided to smear vitamin D3, methylene blue and Ivermectin, it just reinforced my very low opinion of these clowns.
I used to read and watch some of his stuff before he started his "ivermectin is poison" campaign. As soon as he started that- i stopped. There's something not right about it and it makes me wonder how much $ it took for him to smear ivermectin, quercitin, vitamin D, etc...
Big Pharma goal for many decades has been to discredit any treatment module or diagnostic module or nutritional module that is cheap and effective! In the US you don’t become one half Trillion dollar industry any other way! Now custom targeted expensive chemo/cancer treatment and RNA injections will expand the industry to a Trillion dollars!
These desperate and paid confounders are just like roach infestations. I bet they make the same “pop” when stomped on.
A Save The Narrative campaign by the Save Our Asses crew ... as the truth spreads awakening the sleepy-near-dead all efforts - especially censorship as is being passed by complicit U.S. Govt. - are ramped up, to reinforce and beef up the original implanted nonsense. Anything to stop public lynching. Can it be stopped? Time to buy stock in rope's raw material.
Hi Smartest off topic but thought you might like it..
💥
HUMAN CHALLENGE TRIAL FAIL 2024
Scientists tried to give people COVID — and failed
Researchers deliberately infect participants with SARS-CoV-2 in ‘challenge’ trials — but high levels of immunity complicate efforts to test vaccines and treatments.
https://www.nature.com/articles/d41586-024-01284-1
ARCHIVED⬇️
https://archive.md/2024.05.02-115311/https://www.nature.com/articles/d41586-024-01284-1
Yea..They were not smart enough to just target those with impaired immune systems!
All they had to do is check for low Vitamin D and Zinc blood levels!
Read the article. The immune system which is our number one defense against all pathogens kicked in to stop the infection! Daah!
Immunological memory is the ability of the immune system to quickly and specifically recognize an antigen that the body has previously encountered and initiate a corresponding immune response. Generally these are secondary, tertiary and other subsequent immune responses to the same antigen. Immunological memory is responsible for the adaptive component of the immune system, special T and B cells — the so-called memory T and B cells.
.
IgG antibodies are Y-shaped protein molecules that are produced by special white blood cells (B lymphocytes) in response to foreign substances (antigens) such as viruses or bacteria. Antibodies can attach to these viruses or bacteria, rendering them harmless and unable to penetrate healthy cells. They GO AWAY with time and could fall to a NEGATIVE level DOESN'T mean susceptible.
.
Total immunity against viral diseases includes:
1. Local IgA and IgM
2. Humoral immunity of IgG antibodies, both those present in the blood AND those that can be produced quickly when the antigen is present
3. Cellular immunity or MEMORY
4. Other mechanisms.
When we measure antibody titers, we are ONLY documenting the IgG antibodies present in the bloodstream.
.
The Immune System fires up when a pathogen, like a virus, enters the body. The pathogen releases a protein called an antigen, which calls into action the immune system’s special disease-fighting cells. "Called B and T lymphocytes", these cells NOT only destroy the virus, but they REMEMBER what it looked like so they can fend it off in the FUTURE.
.
IMMUNOLOGIC MEMORY allows the immune system to REMEMBER the antigens or organisms to which it has previously been exposed. MEMORY EFFECTOR B cells (long-lived plasma cells) and MEMORY T-cells specific to a virus, give long-term immunity against these diseases.
.
ADAPTIVE IMMUNITY.
.
The “Adaptive Immune Response" is younger than the “Innate Immune Response" in evolutionary terms and is more specific and considerably MORE POTENT in its effects.
.
The constituents of the adaptive immune response are the lymphoid cells. These include:
.
The T lymphocytes and the cytokine and chemokine messenger proteins released by these cells, which direct and REGULATE the adaptive immune response.
.
The B lymphocytes, which transform to the late-stage plasma cells that produce and secrete antibody.
.
The lymphoid cells of the adaptive immune response reside in, and circulate between, the various lymphoid tissues of the body (e.g. the lymph nodes, spleen and mucosal lymphoid tissues). In the adaptive immune response, antigen is first transported from a site of infection by a dendritic cell to the regional lymphoid tissue. That dendritic cell in turn activates "Antigen-Specific T lymphocytes," which further activate Antigen-Specific B lymphocytes.”
.
These activated, Antigen-Specific lymphocytes must then be mobilized from the regional lymphoid tissue and sent to the site of infection, a process that involves these cells moving into the lymphatic and blood circulation and interacting with the endothelial lining of blood vessels.
.
Once these cells reach the site of infection, they are able to mount a full-scale ‘EFFECTOR’ response, which is considerably STRONGER than that permitted by innate immunity. As these processes take some time to occur (in the order of 4–7 days), there is a delay before adaptive immunity ‘takes over’ from the innate form of defence.
.
The final component of Adaptive Immunity is the development of a “REGULATORY RESPONSE" that will "SWITCH OFF" the system when it is NO LONGER REQUIRED (i.e. when the pathogen has been ELIMINATED) so as NOT to cause DAMAGE to normal body tissue.
.
HOWEVER, once this is achieved, the immune system retains the “MEMORY” of that immune response.
IMMUNOLOGICAL MEMORY is another key feature of the Adaptive Immune Response. MEMORY allows the generation of a much MORE effective SECONDARY IMMUNE RESPONSE (Anamnestic MEMORY Response) if that same antigen is EVER RE-ENCOUNTERED.
…
Thank yo! Well explained. Give all physicians a test on this before licensing! So..why does the medicine man not focus on improving immune system response in immune compromised humans.
They are not our friends..
My wife acquired B cell lymphoma. The Mayo researcher said they didn't have a clue why the B Cells attack the T cells that normally stop the viral invasion. Took ten years before the LDH went through the roof.
Used to subscribe to Celia, but then cut it off maybe over a year ago. I don't recall why but something about her writing/viewpoint not being well thought out...
followed her for awhile also but it was short lived. others took me longer but all were lessons learned. honestly, i'm still learning.
I unsubscribed some time last year. It was getting too much for me.
Even I fell for it (and I love Celia). WTF. Propaganda is wicked.
Tim truth been chasing the IVM and Quercetin poisoning for over a year. I tried asking Dr.kory on twitter but I never got a response https://open.substack.com/pub/timtruth/p/poison-alert-dangerous-methylene?r=ykqw5&utm_campaign=post&utm_medium=web
Certainly doesn't seem to have stopped fertility in Africa...
Celia tends to jump on to a topic before she knows if its true.
Saw Celia's article yesterday, was a little surprised about it. Usually she is on top of most things but I don't follow Tim Truth either. Some of the comments on her article are worth the read as well. Linking your article today @https://nothingnewunderthesun2016.com/
Hopefully Celia reads your take as well.
I just saw what he is saying about ivermectin and also fenbenzedole, saying it's cockroach poison. What the fuck is going on, I'm assuming he's a pharma shill, trying to disparage a nobel prize winning drug. It's had billions of doses supplies and I've read it's safer than Panadol, is this true. Someone please help
Why would you need help? Billions of doses administered with virtually no side effects considered safer than tylenol. Clearly this person has an agenda alligned with the Elites that control Pharma "they want you dead" hence treatments that help are disparaged, this same clown also claims Quercetin is dangerous nd no doubt vitamin D and C are "dangerous" do you not see the pattern?
Ivermectin sounds very promising and has received a lot of publicity. However, it is still a Big Pharma product controlled by Big Pharma! I guess the question we have to ask ourselves is why they are still allowing it to be sold on the open market to the masses to use off-label as opposed to Hydroxycholoroquine and other off-label medications that were suggested during the Plandemic? I have zero trust in Big Pharma and the U.S. Medical System!
Ivermectin was first sold on the open market in the early 1980s at a time when pharma was actually producing useful compounds conicidentally Fenbendazole another antiparasitic also came out at that time. Both were initally used as an antiparasitics for animals and later repuprosed for humans. In Fenbendazole's case an entirely neutral sulfur subsititution was deployed and renamed mebendzole so the same thing could be sold for thousands of dollars per dose.
Ivermectin and Fenbendazole research for efficacy in other diseases including antiviral or even anticancer properties typically had good in vitro results good in vivo results (in animals) and then research stopped----Big pharmas mantra No Profit=No Product.
These drugs are now off patent and big pharma has actively tried to prevent them being repurposed for off label use.
Merck went as far as trying to purchase all the Ivermectin production facilities in India that turned into a game of whack a mole as one facility would be bought out and another set up. This has ZERO to do with big pharma who have actively tried to prevent the off label use of these compounds.
So to answer to your question repurposed off patent drugs thankfully are not in big pharma's control as described above. If you want to put big pharma out of business buy these life saving compounds as they represent to big pharma cheaper better products that actually work! Complete antithetical to big pharma's goals.
Thanks for clarifying that, Sid. I understand that they are also touting it as a cure for Cancer; however, I think a much better and much safer alternative to any pharmaceutical is Hemp Oil (composed of THC, CBD, and CBG), not to be confused with Hemp Seed Oil which has the best healing and Cancer curing properties. In his book "Nature's Answer to Cancer" Rick Simpson discusses his frustration with the Canadian medical system in treating his Cancer until he discovered Hemp Oil. Rick Simpson took it upon himself to opt out of conventional therapy with chemo and dangerous Big Pharma drugs and treated himself with his homemade hemp oil. He used his oil to treat thousands of Canadians suffering from Cancer and other serious health issues with his oil for Free. The result was that the Canadian government wanted to put him in prison. That in itself proves how well Hemp Oil works!
CBD oil is one of the components of the new and improved Tippens protocol, but it is not enough on its own.
There is a new full spectrum organic CBD product launching soon on this Substack which will be the most potent offering available, and at the most affordable price-point.
With all due respect, 2nd Smartest Guy, I have witnessed the Rick Simpson Oil for myself work wonders; Rick Simpson documented his results for THC/CBD oil before anyone even knew what CBD oil was. I just started making this oil for myself (circled back to the CBD "wagon") and my wife; it is fantastic. The stuff (junk) on the market is mass-produced and does not use the decarboxylation method to release the actual CBD, THC, CBG, and Terpene profile to get the same effect as the active ingredients in the hemp plant. The stuff on the market is mass-produced and is filtered with olive oil as a carrier. The Hemp has to be stripped of the trichome with either a solvent (200-proof food-grade alcohol), CO2, or Butane. Solvents are the best and then decarboxylated by dissolving the solvent at an optimal temperature without denaturing the CBD, THC, and CBG.
With all due respect IVM is easily one of the safest compounds out there. Given that many dissident Dr's in my case molecular biologist at risk to our careers spoke out about the anticancer properties of this compound "touting" is a really unfair characterization.
That being said it is very naive to think that any single compound is a "magic" bullet. I am a strong proponent of the "warburg" effect that states that cancer cells effectively rely on glucose instead of oxygen to store energy in the form of lactate. By making this in effect a therapeutic target calls for an integrative approach to this disease that includes a sugar restricted diet (I found substituting allulose (a rare sugar that is not metabolized) for regular sugar works great at starving cancer cells.
As a caregiver for a patient who happened to be a close relative I was able to bring stage 3 Multiple myeloma with a grim prognosis of only a few months to 100 percent full remission in seven months much to the chagrin of the Moffit cancer centre that my relative rejected their toxic chemothrapy but I digress,
Several steps were crucial;
1) he loved wine at least a bottle a day so I substituted wine for canaboid Oil being aware of the anticancer properties you refer to and as it was medicinal cannaboid oil that he had to register as a patient in Florida to obtain it helped relieve his anxieties.
2) Keto like diet
3) Fenbendazole 500 Mg daily.
4) Quercetin (konwn anti MM properties 2000 mg a day)
5) Vitamin d3 20000 Iu daily vital for bone health for MM patients Moffit center totally ignored this
This integrative approach worked. Additionally I know of at least one other patient that did a similar course of action except had IVM instead of Quercetin( 24 mg a day.) Also a patient that was at deaths door.
"Magic bullet" approach has a lower probability of working than an integratve approach.
Bravo; that is a beautiful recipe for healing! I am not well versed on the Ivermectin and I was out of the medical industry after twenty four plus years by December of 2020! We were one of the first medical clinics in my area at the time that would provide the medical marijuana recommendations.
I'm assuming you are talking about RSO
Yes, fantastic stuff; I sleep like I did when I was seventeen! Any aches and pains melt away, and stress levels are at zero! The stuff that I use is low in THC 0.5% and the CBD is 17%. Rick Simpson recommends 17% THC for patients with cancers, especially advanced cancers!
Info you all may learn from, too
https://vigilantnews.com/post/sasha-latypova-do-not-comply-with-what-happens-next/